Survival of BRCA1/BRCA2-associated pT1 breast cancer patients, a cohort study.


Journal

Breast cancer research and treatment
ISSN: 1573-7217
Titre abrégé: Breast Cancer Res Treat
Pays: Netherlands
ID NLM: 8111104

Informations de publication

Date de publication:
Jul 2022
Historique:
received: 17 01 2022
accepted: 13 04 2022
pubmed: 5 5 2022
medline: 9 6 2022
entrez: 4 5 2022
Statut: ppublish

Résumé

Intensive screening in BRCA1/2 mutation carriers aims to improve breast cancer (BC) prognosis. Our aim is to clarify the prognostic impact of tumor size in BRCA mutation carriers with a pT1 BC, which is currently unclear. We are especially interested in differences between pT1a, pT1b, and pT1c regarding the prognosis of node-negative breast cancer, the effect of chemotherapy, and the prevalence of lymph node involvement. For this study, BRCA1/2-associated BC patients were selected from a nationwide cohort. Primary outcomes were 10-year overall survival (OS) per pT1a-b-c group and the effect of chemotherapy on prognosis of node-negative BC, using Kaplan-Meier and Cox models. Finally, we evaluated lymph node involvement per pT1a-b-c group. 963 women with pT1 BRCA1/2-associated BC diagnosed between 1990 and 2017 were included, of which 679 had pN0 BC. After a median follow-up of 10.5 years, 10-year OS in patients without chemotherapy was 77.1% in pT1cN0 and lower than for pT1aN0 (91.4%, p = 0.119) and pT1bN0 (90.8%, p = 0.024). OS was better with than without chemotherapy for pT1cN0 (91.6% vs. 77.1%, p = 0.001; hazard ratio (HR) 0.56, 95% confidence interval (CI): 0.21-1.48). Lymph node involvement was 24.9% in pT1c, 18.8% in pT1b, and 8.6% in pT1a. Smaller tumor size is associated with better OS and less lymph node involvement in pT1 BRCA1/2-associated BC patients. The results suggest that early detection in BRCA1/2 mutation carriers of pT1a/b BC may reduce mortality and the need for systemic therapy.

Identifiants

pubmed: 35507134
doi: 10.1007/s10549-022-06608-1
pii: 10.1007/s10549-022-06608-1
pmc: PMC9167195
doi:

Substances chimiques

BRCA1 Protein 0
BRCA1 protein, human 0
BRCA2 Protein 0
BRCA2 protein, human 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

159-170

Informations de copyright

© 2022. The Author(s).

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Auteurs

Mark van Barele (M)

Department of Medical Oncology, Erasmus MC Cancer Institute, University Medical Centre Rotterdam, Rotterdam, The Netherlands.

Amy Rieborn (A)

Department of Medical Oncology, Erasmus MC Cancer Institute, University Medical Centre Rotterdam, Rotterdam, The Netherlands.

Bernadette A M Heemskerk-Gerritsen (BAM)

Department of Medical Oncology, Erasmus MC Cancer Institute, University Medical Centre Rotterdam, Rotterdam, The Netherlands.

Inge-Marie Obdeijn (IM)

Department of Radiology, Erasmus MC Cancer Institute, University Medical Centre Rotterdam, Rotterdam, The Netherlands.

Linetta B Koppert (LB)

Department of Surgical Oncology, Erasmus MC Cancer Institute, University Medical Centre Rotterdam, Rotterdam, The Netherlands.

Claudette E Loo (CE)

Department of Radiology, Division of Diagnostic Oncology, Netherlands Cancer Institute-Antoni van Leeuwenhoek Hospital, Amsterdam, The Netherlands.

Rob A E M Tollenaar (RAEM)

Department of Surgery, Leiden University Medical Centre, Leiden, The Netherlands.

Margreet G E M Ausems (MGEM)

Division Laboratories, Pharmacy and Biomedical Genetics, Department of Genetics, University Medical Centre Utrecht, Utrecht, The Netherlands.

Irma van de Beek (I)

Department of Clinical Genetics, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands.

Lieke P V Berger (LPV)

Department of Genetics, University of Groningen, University Medical Centre Groningen, Groningen, The Netherlands.

Maaike de Boer (M)

Division of Medical Oncology | Department of Internal Medicine, GROW-School of Oncology and Developmental Biology, Maastricht University Medical Centre, Maastricht, The Netherlands.

Liselot P van Hest (LP)

Department of Clinical Genetics, Amsterdam UMC, Vrije Universiteit Amsterdam, De Boelelaan 1117, Amsterdam, The Netherlands.

C Marleen Kets (CM)

Department of Human Genetics, Radboud University Medical Centre, Nijmegen, The Netherlands.

Matti Rookus (M)

Department of Epidemiology, Netherlands Cancer Institute-Antoni Van Leeuwenhoek Hospital, Amsterdam, The Netherlands.

Marjanka K Schmidt (MK)

Division of Molecular Pathology, Netherlands Cancer Institute, Amsterdam, The Netherlands.

Agnes Jager (A)

Department of Medical Oncology, Erasmus MC Cancer Institute, University Medical Centre Rotterdam, Rotterdam, The Netherlands.

Maartje J Hooning (MJ)

Department of Medical Oncology, Erasmus MC Cancer Institute, University Medical Centre Rotterdam, Rotterdam, The Netherlands. m.hooning@erasmusmc.nl.

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Classifications MeSH